Trace Elements Associated with Systemic Lupus Erythematosus and Insulin Resistance.


Journal

Biological trace element research
ISSN: 1559-0720
Titre abrégé: Biol Trace Elem Res
Pays: United States
ID NLM: 7911509

Informations de publication

Date de publication:
Sep 2019
Historique:
received: 27 11 2017
accepted: 27 11 2018
pubmed: 3 1 2019
medline: 25 12 2019
entrez: 3 1 2019
Statut: ppublish

Résumé

Systemic lupus erythematosus (SLE) is a chronic inflammatory autoimmune disease of multifactorial origin. Studies have shown that trace elements such as zinc and copper may help maintain optimum function of the immune system and metabolism, while toxic metals such as lead may increase systemic autoimmunity. The current study aimed to assess the relationship between serum concentration of lithium (Li), vanadium (V), copper (Cu), zinc (Zn), molybdenum (Mo), cadmium (Cd), and lead (Pb) and SLE diagnosis, disease activity measured by SLE disease activity index (SLEDAI) and insulin resistance (IR). This case-control, cross-sectional study included 225 patients, 120 healthy controls, and 105 SLE patients. Serum concentration of Li, V, Cu, Zn, Mo, Cd, and Pb was measured. Serum concentrations of V (p < 0.001), Zn (p < 0.001), and Pb (p < 0.001) were lower and Mo (p < 0.001) and Li (p < 0.001) were higher in patients with SLE compared to healthy controls. SLE diagnosis was associated with higher serum Li (p < 0.001) concentration and lower V (p < 0.001), Zn (p = 0.003), and Pb (p = 0.020). Toxic metals and trace elements were not associated with disease activity. Levels of Cd were higher in patients with IR (p = 0.042). There was no significant association between IR and the other metals. The results indicate that SLE patients have different profiles of trace elements and toxic metals compared to healthy controls. While some toxic metals and trace elements were found to be associated with SLE diagnosis, they had no effect on disease activity and IR.

Identifiants

pubmed: 30600500
doi: 10.1007/s12011-018-1592-7
pii: 10.1007/s12011-018-1592-7
doi:

Substances chimiques

Trace Elements 0

Types de publication

Clinical Trial Comparative Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

34-44

Auteurs

Eliel Marcio Pedro (EM)

Department of Chemistry, University of Londrina, Londrina, Paraná, Brazil.

Lorena Flor da Rosa Franchi Santos (LF)

Research Laboratory of Applied Immunology, University of Londrina, Paraná, Brazil.

Bruna Miglioranza Scavuzzi (BM)

Research Laboratory of Applied Immunology, University of Londrina, Paraná, Brazil.

Tatiana Mayumi Veiga Iriyoda (TMV)

Department of Rheumatology, Pontifícia Universidade Católica, PUC, Londrina, Paraná, Brazil.

Tiago Severo Peixe (TS)

Department of Pathology, Clinical Analysis and Toxicology, University of Londrina, Rua Robert Koch, n 60, Londrina, Paraná, Brazil.

Marcell Alysson Batiste Lozovoy (MAB)

Department of Pathology, Clinical Analysis and Toxicology, University of Londrina, Rua Robert Koch, n 60, Londrina, Paraná, Brazil.

Edna Maria Vissoci Reiche (EMV)

Department of Pathology, Clinical Analysis and Toxicology, University of Londrina, Rua Robert Koch, n 60, Londrina, Paraná, Brazil.

Isaias Dichi (I)

Department of Internal Medicine, University of Londrina, Londrina, Paraná, Brazil.

Andréa Name Colado Simão (ANC)

Department of Rheumatology, Pontifícia Universidade Católica, PUC, Londrina, Paraná, Brazil. deianame@yahoo.com.br.
Department of Pathology, Clinical Analysis and Toxicology, University of Londrina, Rua Robert Koch, n 60, Londrina, Paraná, Brazil. deianame@yahoo.com.br.

Maria Josefa Santos (MJ)

Department of Pathology, Clinical Analysis and Toxicology, University of Londrina, Rua Robert Koch, n 60, Londrina, Paraná, Brazil.

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Classifications MeSH